In school-aged children with cystic fibrosis (CF) structural lung damage assessed using chest CT is associated with abnormal ventilation distribution. The primary objective of this analysis was to determine the relationships between ventilation distribution outcomes and the presence and extent of structural damage as assessed by chest CT in infants and young children with CF., respectively]), chest CT and airway pathology from bronchoalveolar lavage were determined at diagnosis and then annually. The chest CT scans were evaluated for the presence or absence of bronchiectasis and air trapping.. There was a weak, but statistically significant association between the extent of air trapping and all ventilation distribution outcomes.These findin...
BACKGROUND: In cystic fibrosis (CF), irreversible lung disease arises in early life, and is often as...
AbstractBackgroundThe quality of chest Computed Tomography (CT) images in children is dependent upon...
BACKGROUND: Accelerated lung function decline in individuals with cystic fibrosis (CF) starts in ado...
In school-aged children with cystic fibrosis (CF) structural lung damage assessed using chest CT is ...
BACKGROUND: In school-aged children with cystic fibrosis (CF) structural lung damage assessed using ...
Background: In school-aged children with cystic fibrosis (CF) structural lung damage assessed using ...
Introduction: Mosaic attenuation on expiratory chest computed tomography (CT) is common in early lif...
Rationale: The lung clearance index is a measure of ventilation distribution derived from the multip...
International audienceChest tomography (CT) using the controlled ventilation technique (CTCV) is a s...
Background: Infants with cystic fibrosis (CF) develop structural lung disease early in life, and vir...
Background: Computed tomography (CT) of the lungs is the gold standard for assessing the extent of s...
Objective: The aim of this study was to determine whether assessment of early CT scan-detected bronc...
Objective To examine the distribution of early structural lung changes in clinically stable infants ...
© 2014 Dr. Anne-Marie EbdonAir-trapping is frequently identified in infants with cystic fibrosis (CF...
Rationale: The promise of newborn screening (NBS) for cystic fibrosis (CF) has not been fully realiz...
BACKGROUND: In cystic fibrosis (CF), irreversible lung disease arises in early life, and is often as...
AbstractBackgroundThe quality of chest Computed Tomography (CT) images in children is dependent upon...
BACKGROUND: Accelerated lung function decline in individuals with cystic fibrosis (CF) starts in ado...
In school-aged children with cystic fibrosis (CF) structural lung damage assessed using chest CT is ...
BACKGROUND: In school-aged children with cystic fibrosis (CF) structural lung damage assessed using ...
Background: In school-aged children with cystic fibrosis (CF) structural lung damage assessed using ...
Introduction: Mosaic attenuation on expiratory chest computed tomography (CT) is common in early lif...
Rationale: The lung clearance index is a measure of ventilation distribution derived from the multip...
International audienceChest tomography (CT) using the controlled ventilation technique (CTCV) is a s...
Background: Infants with cystic fibrosis (CF) develop structural lung disease early in life, and vir...
Background: Computed tomography (CT) of the lungs is the gold standard for assessing the extent of s...
Objective: The aim of this study was to determine whether assessment of early CT scan-detected bronc...
Objective To examine the distribution of early structural lung changes in clinically stable infants ...
© 2014 Dr. Anne-Marie EbdonAir-trapping is frequently identified in infants with cystic fibrosis (CF...
Rationale: The promise of newborn screening (NBS) for cystic fibrosis (CF) has not been fully realiz...
BACKGROUND: In cystic fibrosis (CF), irreversible lung disease arises in early life, and is often as...
AbstractBackgroundThe quality of chest Computed Tomography (CT) images in children is dependent upon...
BACKGROUND: Accelerated lung function decline in individuals with cystic fibrosis (CF) starts in ado...